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FGFRL1 Gene Radioulnar Synostosis FGFRL1 Related Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The FGFRL1 gene plays a crucial role in bone development and growth. Mutations in this gene can lead to a condition known as radioulnar synostosis, where the radius and ulna bones in the forearm are fused together, limiting movement and leading to a range of mobility issues. To identify the presence of mutations in the FGFRL1 gene that could cause this condition, a specialized genetic test is available at DNA Labs UAE.

This test is designed to analyze the FGFRL1 gene for any abnormalities that might result in radioulnar synostosis. By detecting these mutations, healthcare providers can confirm a diagnosis, allowing for appropriate management and treatment plans to be developed. The test is particularly valuable for individuals showing symptoms of the condition or those with a family history of radioulnar synostosis, as it provides a clear genetic basis for the disorder.

The cost of the FGFRL1 related genetic test at DNA Labs UAE is 4400 AED. This price includes the collection of a DNA sample, usually through a blood draw or cheek swab, the genetic analysis in the laboratory, and a comprehensive report of the findings. The test is performed under strict quality control measures to ensure accurate and reliable results. Patients considering this test are advised to consult with a healthcare professional or genetic counselor to understand the implications of the results and discuss potential next steps in care or treatment.

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FGFRL1 Gene Radioulnar synostosis FGFRL1 related Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering advanced genetic testing services. In this blog, we will discuss the FGFRL1 Gene Radioulnar synostosis FGFRL1 related Genetic Test, including its cost, symptoms, diagnosis, and test details.

Test Name: FGFRL1 Gene Radioulnar synostosis FGFRL1 related Genetic Test

Components:

  • Price: 4400.0 AED

Sample Condition:

Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery:

3 to 4 Weeks

Method:

NGS Technology (Next-Generation Sequencing)

Test Type:

Osteology Dermatology Immunology Disorders

Doctor:

Dermatologist

Test Department:

Genetics

Pre Test Information:

Clinical History of Patient who is going for FGFRL1 Gene Radioulnar synostosis, FGFRL1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFRL1 Gene Radioulnar synostosis, FGFRL1 related NGS Genetic DNA Test gene FGFRL1

Test Details:

FGFRL1 Gene Radioulnar synostosis is a genetic condition characterized by the fusion of the radius and ulna bones in the forearm. This fusion restricts the movement of the forearm, leading to limited rotation and pronation/supination. A FGFRL1 related NGS genetic test is a type of genetic test that analyzes the FGFRL1 gene for any mutations or variations that may be associated with Radioulnar synostosis. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology used to rapidly analyze multiple genes simultaneously. By analyzing the FGFRL1 gene, this genetic test can identify any mutations or variations that may be responsible for Radioulnar synostosis. This information can be helpful in diagnosing the condition, understanding its inheritance pattern, and providing appropriate genetic counseling to affected individuals and their families. Genetic testing can also be beneficial in prenatal diagnosis for families with a known FGFRL1 gene mutation, allowing them to make informed decisions about their pregnancy and plan for appropriate medical management. It is important to note that genetic testing should be done under the guidance of a qualified healthcare professional who can interpret the results and provide appropriate counseling and support.

Test Name FGFRL1 Gene Radioulnar synostosis FGFRL1 related Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FGFRL1 Gene Radioulnar synostosis, FGFRL1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFRL1 Gene Radioulnar synostosis, FGFRL1 related NGS Genetic DNA Test gene FGFRL1
Test Details

FGFRL1 Gene Radioulnar synostosis is a genetic condition characterized by the fusion of the radius and ulna bones in the forearm. This fusion restricts the movement of the forearm, leading to limited rotation and pronation/supination.

A FGFRL1 related NGS genetic test is a type of genetic test that analyzes the FGFRL1 gene for any mutations or variations that may be associated with Radioulnar synostosis. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology used to rapidly analyze multiple genes simultaneously.

By analyzing the FGFRL1 gene, this genetic test can identify any mutations or variations that may be responsible for Radioulnar synostosis. This information can be helpful in diagnosing the condition, understanding its inheritance pattern, and providing appropriate genetic counseling to affected individuals and their families.

Genetic testing can also be beneficial in prenatal diagnosis for families with a known FGFRL1 gene mutation, allowing them to make informed decisions about their pregnancy and plan for appropriate medical management.

It is important to note that genetic testing should be done under the guidance of a qualified healthcare professional who can interpret the results and provide appropriate counseling and support.

SKU: TEST-3235 Category:

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